Abstract

Herein, we report on the efficient visible-light driven BiPW12O40/BiOI (BPWBI) photocatalyst that was prepared by combining different weight percentages of BiPW12O40 (1.0, 3.0, 5.0%) with BiOI via facile one–step wet impregnation method. The prepared BPWBI photocatalysts were characterized by XRD, FTIR, TGA, BET, FESEM, EDS/Mapping, TEM, UV–Vis DRS, and PL. The photocatalytic performance of the materials was assessed for the degradation of Bisphenol A (BPA) under visible light. The optimum composite photocatalyst (1.0BPWBI) exhibited an efficiency of 94.2% on BPA after 120 min at the optimum conditions (catalyst dosage = 20 mg, pH = 6.68, and constant pollutant concentration = 15 mg L−1). In the presence of peroxodisulfate (PDS), the efficiency was improved to 98.7% in 80 min whereas the efficiency was drastically reduced in the presence of acid blue 25 (AB 25) dye. Photoluminescence (PL) measurements, confirmed that 1.0BPWBI exhibited enhanced electron-hole separation and slow recombination rate of electron-hole pairs. The trapping experiments deduced that h+, and O2− were the most active species responsible for the degradation of BPA. Moreover, the photodegradation pathway was hypothesized based on the LC-MS results on transformation products in the presence of 1.0BPWBI. The impressive photocatalytic performance and stability proved that 1.0BPWBI catalyst renders itself as a promising and valuable photocatalyst for wastewater treatment and can be further explored in the degradation of other organic pollutants for environmental remediation.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.